3.8 Article

Dram1 regulates DNA damage-induced alternative autophagy

期刊

CELL STRESS
卷 2, 期 3, 页码 55-65

出版社

SHARED SCIENCE PUBLISHERS OG
DOI: 10.15698/cst2018.03.127

关键词

alternative autophagy; DNA damage response; genotoxic stress; p53; Dram1

资金

  1. MEXT of Japan [17H01533, 17H06414, 16K15230, 17H05691, 15K19004]
  2. Project for Cancer Research and Therapeutic Evolution (P -CREATE)
  3. Project for Psychiatric and Neurological Disorders from the Japan Agency for Medical Research and Development, AMED
  4. Joint Usage/Research Program of Medical Research Institute, Tokyo Medical and Dental University
  5. Takeda Science Foundation
  6. Grants-in-Aid for Scientific Research [16K15230, 15K19004, 26110005, 17K08649, 17H01533, 15K08420, 17H06413, 17H06414, 17H05691] Funding Source: KAKEN

向作者/读者索取更多资源

Autophagy is an evolutionarily conserved process that degrades subcellular constituents. Mammalian cells undergo two types of autophagy; Atg5-dependent conventional autophagy and Atg5-independent alternative autophagy, and the molecules required for the latter type of autophagy are largely unknown. In this study, we analyzed the molecular mechanisms of genotoxic stress-induced alternative autophagy, and identified the essential role of p53 and damage-regulated autophagy modulator (Dram1). Dram1 was sufficient to induce alternative autophagy. In the mechanism of alternative autophagy, Dram1 functions in the closure of isolation membranes downstream of p53. These findings indicate that Dram1 plays a pivotal role in genotoxic stress-induced alternative autophagy.

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